Effect of a bacteriocin-producing Streptococcus salivarius on the pathogen Fusobacterium nucleatum in a model of the human distal colon

ABSTRACT The gut microbiome is a vast reservoir of microbes, some of which produce antimicrobial peptides called bacteriocins that may inhibit specific bacteria associated with disease. Fusobacterium nucleatum is an emerging human bacterial pathogen associated with gastrointestinal diseases including colorectal cancer (CRC). In this study, fecal samples of healthy donors were screened for potential bacteriocin-producing probiotics with antimicrobial activity against F. nucleatum. A novel isolate, designated as Streptococcus salivarius DPC6993 demonstrated a narrow-spectrum of antimicrobial activity against F. nucleatum in vitro. In silico analysis of the S. salivarius DPC6993 genome revealed the presence of genes involved in the production of the bacteriocins salivaricin A5 and salivaricin B. After 6 h in a colon fermentation model, there was a significant drop in the number of F. nucleatum in samples that had been simultaneously inoculated with S. salivarius DPC6993 + F. nucleatum DSM15643 compared to those inoculated with F. nucleatum DSM15643 alone (mean ± SD: 9243.3 ± 3408.4 vs 29688.9 ± 4993.9 copies/μl). Furthermore, 16S rRNA amplicon analysis revealed a significant difference in the mean relative abundances of Fusobacterium between samples inoculated with both S. salivarius DPC6993 and F. nucleatum DSM15643 (0.05%) and F. nucleatum DSM15643 only (0.32%). Diversity analysis indicated minimal impact exerted by S. salivarius DPC6993 on the surrounding microbiota. Overall, this study highlights the ability of a natural gut bacterium to target a bacterial pathogen associated with CRC. The specific targeting of CRC-associated pathogens by biotherapeutics may ultimately reduce the risk of CRC development and positively impact CRC outcomes.


Introduction
The gastrointestinal tract (GI) harbors trillions of diverse microbes, including candidate biotherapeutic bacteria such as probiotics. Probiotic bacteria are defined as "live microorganisms that, when administered in adequate amounts, confer a health benefit on the host". 1 Probiotic bacteria can exert health benefits on its host through several mechanisms, including targeting pathogenic microbes via antimicrobial production. 2 Therefore, the GI tract has been regarded as a reservoir for novel antimicrobials, and extensive research has been focused on screening bacterial gut isolates for antimicrobial compounds such as bacteriocins. 3,4 Bacteriocins are antimicrobial peptides produced by specific bacteria, which exhibit potent activity against other bacteria. 5 It should be noted that the in vitro inhibitory activity of bacteriocins against a particular target does not necessarily translate to the gut environment. Ex vivo models provide a convenient means of bridging the gap between in vitro and in vivo investigations to assess the impact of different modulators on the gut microbiota. 6,7 Indeed, ex vivo models of the colon have been used on a number of occasions to evaluate the impact of antibiotics 8 and bacteriocins 9,10 on intestinal microbial communities.
The role of the gut microbiota in colorectal cancer (CRC) has been the focus of ever increasing interest and a number of bacterial species have recently been associated with the disease. 11,12 Fusobacterium nucleatum is an emerging pathogen shown to be associated with many GI diseases but specifically with CRC, where high abundances of Fusobacterium and F. nucleatum have been identified in colon cancer samples by transcriptomic and metagenomic profiling, in comparison to healthy controls. [13][14][15][16][17][18][19] Indeed, there is now increasing evidence to suggest that the association between F. nucleatum and CRC reflects causation rather than correlation, 20,21 thus making F. nucleatum a potential therapeutic target for prevention of this disease. Targeting specific species associated with CRC, while exerting minimal impact on the surrounding microbiota, is an attractive proposition and, thus, narrow-spectrum antimicrobials, such as bacteriocins, are particularly relevant.
The genus Streptococcus comprises some healthpromoting members including strains of the species Streptococcus salivarius. These healthpromoting attributes have been identified in the S. salivarius M18 22 strain and the commercially available bacteriocin-producing S. salivarius K12 strain. S. salivarius K12 exerts narrow-spectrum antimicrobial activity against Streptococcus pyogenes, 23 an oral pathogen associated with many oral pathologies including pharyngitis. S. salivarius K12 has shown promise for the treatment of oral streptococcal diseases in numerous clinical trials 24 and may also have health benefits at other body sites. 25 On the basis of this evidence, there is merit in investigating the application of other S. salivarius strains for health promoting purposes. Here, we screened fecal samples of healthy donors and isolated a potential bacteriocin-producing probiotic designated S. salivarius DPC6993 with antimicrobial activity against F. nucleatum. Then, we investigated the impact of S. salivarius DPC6993 on F. nucleatum in an ex vivo model of the human colon.

Screening and isolation of bacteriocin-producing bacteria
A large-scale screen for antimicrobial activity against F. nucleatum was performed using agarbased deferred antagonism assays. Screening of over 16,000 colonies from 17 fecal samples from a cohort of healthy donors resulted in the detection of 56 colonies exhibiting antimicrobial activity against F. nucleatum DSM15643. This number was subsequently reduced to five isolates following repeat overlay assays (to ensure the retention of this initial phenotype) and well assays with buffered and unbuffered cell-free supernatant (in order to rule out inhibitory activity due to organic acid production). 16S rRNA gene sequencing established that all of the five isolates were speciated as S. salivarius. A single isolate was taken forward for further characterization and designated S. salivarius DPC6993.

Antimicrobial-producing capacity of S. salivarius DPC6993
Following genome sequencing of S. salivarius DPC6993, the draft genome was screened for the presence of genes that encode putative antimicrobial peptides, specifically bacteriocins, using the software BAGEL3, an automated bacteriocin mining tool. 26 Analysis revealed two putative bacteriocin clusters corresponding to salivaricin B 27 and salivaricin A5 28 bacteriocins, confirmed by multiple sequence alignments on Clustal Omega. 29 The sequences of the predicted structural peptides of the two clusters had 100% amino acid identity with these salivaricins (Figure 1a  Initially, S. salivarius DPC6993 demonstrated antimicrobial activity against F. nucleatum DSM15643 ( Figure 3) and Lactobacillus delbrueckii subsp. bulgaricus DPC5383 producing zones of 5-8 mm and 8-10 mm, respectively. The spectrum of activity of S. salivarius DPC6993 against a panel of bacterial strains representing those typically found in the mammalian gastrointestinal and urogenital tracts was further tested (Table S2) (Table S2).

Impact of the bacteriocin-producing S. salivarius DPC6993 on F. nucleatum in a model colonic environment
To determine the impact of the bacteriocinproducer S. salivarius DPC6993 on F. nucleatum DSM15643 numbers in a simulated colon environment, the two strains were inoculated into such an environment at 10 9 and 10 6 CFU/ml, respectively. Quantification of F. nucleatum was performed by real time-quantitative polymerase chain reaction (RT-qPCR) on DNA extracted from all colon model wells at time points T0, T6 and T24 postinoculation. Four variations were studied: S. salivarius DPC6993 with F. nucleatum DSM15643; S. salivarius DPC6993 only; F. nucleatum DSM15643 only and controls (blank fecal slurry) ( Figure 4). Studies were performed in triplicate for each condition and represented by the mean copy of F. nucleatum ± SD. The qPCR analysis revealed that after 6 h (T6), there was a significant drop in the numbers of F. nucleatum in samples that had been simultaneously inoculated with S. salivarius DPC6993 + F. nucleatum DSM15643 compared to those inoculated with F. nucleatum DSM15643 alone (9243.3 ± 3408.4 vs 29688.9 ± 4993.9 Fn copies/μl, p = .00034) (Figure 4). At T0, there was a significant difference (p = .001) when comparing F. nucleatum numbers between colon model wells inoculated with S. salivarius DPC6993 and F. nucleatum DSM15643 vs inoculated with F. nucleatum DSM15643 only (4452.8 ± 1547.2 vs 7437.9 ± 1650.7 Fn copies/μl). The significant difference observed here may be due to the dominance of S. salivarius DPC6993 and rapid bacteriocin induction when exposed to F. nucleatum. When F. nucleatum DSM15643 only, was injected into the colon model, a fourfold increase was observed after 6 h (T6) (7437.9 ± 1650.7 to 29688.9 ± 4993.9 Fn copies/μl). However, when both F. nucleatum DSM15643 and S. salivarius DPC6993 strains were simultaneously injected into the colon model, just a 2.1-fold increase in F. nucleatum numbers was observed (4452.8 ± 1547.2 to 9243.3 ± 3408.4 Fn copies/μl). After 24 h (T24), F. nucleatum was depleted in all colon model wells. It was noted that F. nucleatum was also detected in wells inoculated with S. salivarius DPC6993 only and control wells at low levels across all timepoints, indicating low levels of F. nucleatum already naturally present in the standardized fecal inoculum (Table S3).

Impact of S. salivarius DPC6993 on fecal bacterial diversity
The impact of introducing the bacteriocin producer on the overall diversity of bacterial populations in the colon was also investigated. To assess the impact on beta diversity, multidimensional scaling (MDS) plots were generated based on the Bray-Curtis Dissimilarity method. The MDS plot based on the calculated distance matrices shows no clustering by treatment or timepoint, indicating no difference in microbial diversity ( Figure 5). The Adonis analysis was not significant when calculated for treatment (p = .237) or timepoint (p = .198).
Alpha diversity metrics were calculated to evaluate the diversity within colon model wells. There were no significant differences in the number of observed genera within timepoints between colon model treatments and controls, except for wells inoculated with F. nucleatum DSM15643 vs control at T6 (p = .03) (Table 1; Figure S1). Shannon and Simpson diversity, reflective of richness and evenness of genera were similar at T0 for all treatments and decreased at T6 and T24 in S. salivarius DPC6993 + F. nucleatum DSM15643 and S. salivarius DPC6993 wells (Table 1). Alpha diversity was significantly higher in F. nucleatum DSM15643 and control wells compared to S. salivarius DPC6993 + F. nucleatum DSM15643 and S. salivarius DPC6993 wells as determined by Simpson and Shannon indices at T6 and T24 (Table 1; Figure S1). However, there were no significant differences in S. salivarius DPC6993 + F. nucleatum DSM15643 (Shannon p = .84; Simpson p = .74) and S. salivarius DPC6993 (Shannon p = .58; Simpson p = .48) wells at T6 compared to T24 indicating that the alpha diversity remained stable and that the initial differences were driven by the dominance of S. salivarius DPC6993 cells (Table 1; Figure S1). F nucleatum DSM15643 and control wells diversity measures remained similar over the 24 h period. Both Shannon and Simpson metrics for all wells at T24 were similar to T6 (Table 1; Figure S1).

Impact of S. salivarius DPC6993on intestinal bacterial populations
To determine the impact of S. salivarius DPC6993 on the composition of the model colonic microbiota, metagenomic DNA was extracted from the model colon samples at T0, T6 and T24 for all treatments and subjected to 16S rRNA sequencing to determine relative abundance of microbial communities. At the phylum level, the most dominant phyla in all colon model treatments across all timepoints were Firmicutes and Actinobacteria with smaller proportions of Proteobacteria, Bacteroidetes and Fusobacteria (Figure 6a). At T6, all colon model wells show an increase in Proteobacteria with a decrease in Firmicutes populations, however a larger increase in Proteobacteria was found in F. nucleatum DSM15643 and control wells relative to the S. salivarius DPC6993 + F. nucleatum DSM15643 and S. salivarius DPC6993 wells (2.7% and 3.3% vs 24.5% and 25.4%, respectively), which may suggest S. salivarius' ability to control Proteobacteria taxa. At T24, proportions of the main phyla remain similar to T6 in all treatments, with abundances of Proteobacteria subsiding (Figure 6a; Table S4).
As the qPCR data demonstrated that S. salivarius DPC6993 may supress the growth of F. nucleatum within a simulated colon environment, we further hypothesized that there would be a decrease in taxa assigned to Fusobacteria and Fusobacterium in colon model wells inoculated simultaneously with S. salivarius DPC6993 and F. nucleatum DSM15643 compared to wells inoculated with F. nucleatum DSM15643 only. Fusobacteria abundances remained similar at T6 relative to T0 in the S. salivarius DPC6993 + F. nucleatum DSM15643 wells (0.05-0.05%) with a slight decrease in the S. salivarius DPC6993 wells (0.058-0.014%); however, abundances increased in the F. nucleatum DSM15643 wells (0.13-0.34%), suggesting S. salivarius' potential to suppress the growth of fusobacterial taxa (Figure 6a). No reads were assigned to Fusobacteria at T24 in all treatments or at T0 and T6 in the control wells. Figure 7 shows a significant difference in the relative abundances of Fusobacterium between colon model wells inoculated with both S. salivarius DPC6993 and F. nucleatum DSM15643 and F. nucleatum DSM15643 only. A 2.7-fold increase (0.12-0.32%) in Fusobacterium relative abundance is observed at T6 in wells inoculated with F. nucleatum DSM15643, compared to no change in Fusobacterium relative abundances at 0.05% when inoculated with S. salivarius DPC6993 at T6. At T24, no reads were assigned to Fusobacterium in colon model wells for either treatments.

Discussion
The gut microbiota can be regarded as a reservoir of novel antimicrobials, including bacteriocins 3 and the potential use of biotherapeutic bacteria, such as bacteriocin-producing probiotics, to target colorectal cancer-associated taxa has been proposed. 31 Probiotics that produce bacteriocins have the potential to be utilized for the elimination of specific microbial pathogens, harnessing a narrow spectrum of activity, leaving the natural microbiota unharmed. 5,32 The association of F. nucleatum and CRC is well established. 13 Several studies highlight its overrepresentation in the tissue and stool samples of CRC patients, 14,17,33,34 therefore identifying F. nucleatum as a therapeutic target. As F. nucleatum was first characterized as a dental pathogen, it is notable that a number of studies have shown the potential use of antimicrobial-producing bacteria [35][36][37] and bacteria isolated from functional foods 38 to inhibit it and other oral pathogens in vitro. The potential use of strains from the fermented milk, kefir, to inhibit  F. nucleatum in vitro has also been noted. 39 Recently, in a study which screened the athlete gut microbiome for antimicrobial-producers, two bacteriocinproducing strains of Enterococcus faecalis were isolated which demonstrated anti-F. nucleatum activity in lab media. 4 Furthermore, probiotic interventional trials aimed at modifying the CRC-associated microbiota have caused a reduction in CRC-associated taxa including Fusobacterium 40,41 ; however, there is limited evidence on targeting specific species associated with the disease within the CRC microbiome. These previous studies show that bacteria with anti-F. nucleatum activity in vitro exist and intervention trials show promise for probiotic bacteria to manipulate CRC-associated taxa. Moreover, targeting specific bacterial species associated with CRC development in the guts of healthy populations, while exerting minimal impact on the surrounding gut microbiota is desirable, and may contribute as a preventative strategy. 31 The aim of the current study was to screen fecal samples of healthy donors for potential bacteriocin-producing isolates that demonstrated narrow-spectrum antimicrobial activity against F. nucleatum, and to subsequently confirm this activity in an ex vivo model of the human colon.
We first screened fecal samples of healthy donors for potential bacteriocin-producing isolates active against F. nucleatum. Following screening of 16,000 colonies and repeat antimicrobial assays, five candidate isolates were further studied. All five isolates were identified as S. salivarius by 16S rRNA gene sequencing. Again, repeat assays were performed which distinguished a single isolate with consistent antimicrobial activity against F. nucleatum and was subsequently given the strain designation S. salivarius DPC6993. Bioinformatic analysis and colony mass spectrometry confirmed the presence of two putative bacteriocin clusters on the genome of S. salivarius DPC6993, salivaricin A5 28 and salivaricin B. 27 Indeed, the species S. salivarius produces many other salivaricin variants and subtypes including salivaricin D, salivaricin E, and salivaricin 9. 42 The use of S. salivarius as a beneficial bacterium has been widely studied and its potential health-promoting characteristics are especially evident by the commercial bacteriocinproducing probiotic strain S. salivarius K12. 24,43 Several other strains of S. salivarius have been identified with antimicrobial activity against pathogenic bacteria, which is attributed to their bacteriocin arsenal. For example, S. salivarius strains HSISS4, YU10 or NU10 demonstrated antimicrobial activity in vitro against Staphylococcus aureus, enterococci, Listeria monocytogenes, Micrococcus luteus and related pathogenic species Streptococcus pyogenes, and Streptococcus mutans. 30,44 Interestingly, a recent study found that, while salivaricin producing strains S. salivarius K12 and M18 did not inhibit F. nucleatum in vitro, both strains were able to co-aggregate with F. nucleatum and inhibit IL-6 and IL-8 secretion. 45 However, we recently reported a novel nisin variant designated as nisin G produced by S. salivarius DPC6487 with in vitro antimicrobial activity against F. nucleatum and other streptococci. 46 While these benefits show potential for targeting pathogenic bacteria associated with disease, several studies show additional potential benefits of S. salivarius, which may impact the gut, including anti-inflammatory properties 47 and maintaining microbial homeostasis. 25 This study showed that S. salivarius DPC6993 had a narrow spectrum of activity in vitro, against Fusobacterium species, including the CRCassociated F. nucleatum, therefore, confirming direct inhibition, having no activity against strains of the genera Lactobacillus (except for Lactobacillus delbruekii subsp. bulgaricus), Enterococcus, Streptococcus, Bacteroides, Clostridium, Listeria, Salmonella, Staphylococcus, Porphymoronas, Atopobium and Gardnerella. The identification of narrow-spectrum antimicrobials, is especially warranted, as the use of broad-spectrum antimicrobials creates a window for opportunistic pathogens to colonize the gut microbiome. 48 As the inhibition of pathogenic bacteria does not necessarily translate beyond in vitro tests, we investigated the ability of S. salivarius DPC6993 to impact the growth of F. nucleatum in an ex vivo model of the human colon. This model simulates the complex and dynamic environment of the colon and, thus, provides an insight into the functionality of the antimicrobial within the human colon prior to human studies. 7 An approach involving the preparation of a fecal standard 49 was used to simulate the distal colon environment, and we used qPCR which is a much more sensitive approach to capture bacteria at low relative abundance and is preferable for the quantification of single species 50 and 16S rRNA sequencing which are considered as complementary and reliable for microbiota profiling. 51 Considering that S. salivarius DPC6993 was isolated from the human gut, it was postulated that it would be active against F. nucleatum in its natural environment. Indeed, this was evident as determined by qPCR, which showed a significant reduction in the growth of F. nucleatum when F. nucleatum DSM15643 was inoculated simultaneously with S. salivarius DPC6993 into a simulated colon environment compared to when inoculated individually. Further to this, it is evident from the 16S rRNA compositional analysis that the CRC-associated genus Fusobacterium is less abundant in colon model wells inoculated with S. salivarius DPC6993 and F. nucleatum DSM15643 relative to wells inoculated with F. nucleatum DSM15643 only.
The 16S rRNA compositional analysis revealed changes in the taxonomic profiles by addition of high numbers of S. salivarius DPC6993 cells. However, the presence of dominant fecal genera in control wells was also observed in S. salivarius DPC6993-treated wells at lower relative abundances across each timepoint, indicating dominance of S. salivarius rather than negatively impacting the surrounding microbiota. Notably, Streptococcus rapidly increased in S. salivarius DPC6993-treated wells to become the most dominant taxa compared to controls after 6 h and remained constant after 24 h. This indicates S. salivarius' ability, to not only survive but to flourish in the harsh conditions of human colon environment. Surviving passage through the GI tract and remaining functional is a desirable characteristic of candidate probiotics. 52 We also investigated how the presence of the bacteriocin-producing S. salivarius DPC6993 impacts on the overall diversity and richness in the colon model. Analysis of beta diversity by multidimensional scaling showed no clustering of datapoints by treatment or timepoint indicating no dramatic change in microbial composition. Alpha diversity reduced in the S. salivarius DPC6993treated wells after 6 h fermentation; however, diversity did not change from 6 to 24 h, indicating that the initial differences were driven by the dominance of S. salivarius DPC6993 cells. Furthermore, there were no significant differences in the number of observed genera between colon model treatments and controls after 24 h fermentation, indicating the microbial richness remained stable. Overall, these results show that the bacteriocin-producing S. salivarius DPC6993 suppresses the growth of F. nucleatum in an ex vivo model of the human colon and exerts minimal impact on the overall diversity of the surrounding microbiota.

Conclusion
This study used an ex vivo model of the human colon to investigate, for the first time, the impact of the bacteriocin-producing S. salivarius DPC6993 on F. nucleatum, a gut pathogen associated with CRC. Results indicate that S. salivarius DPC6993 suppresses the growth of the CRC-associated bacteria within the gut environment and exerts minimal impact on the surrounding gut microbiota. This study is an important finding prior to in vivo analysis to evaluate the potential use of such bacteriocin-producing strains as biotherapeutics for suppressing the growth of F. nucleatum in the human gut, ultimately reducing the risk of CRC development and positively impacting CRC outcomes.

Bacterial strains and cultivation media
S. salivarius DPC6993 was cultivated under anaerobic conditions at 37°C in brain heart infusion (BHI, Difco Laboratories, Detroit, MI, USA) broth and medium. Agar of concentration 1.5% w/v was added for agar plates. F. nucleatum DSM15643 was the target organism used in this study. F. nucleatum DSM15643 was cultivated under anaerobic conditions at 37°C on fastidious anaerobe agar (FAA; Lab M, Lancashire, UK) supplemented with 7% defibrinated horse blood (Cruinn, Dublin, Ireland) and Wilkin-Chalgren Broth (WCB; Oxoid, Hampshire, UK). Both strains were grown anaerobically using anaerobic jars, Anaerocult A gas packs (Merck, Darmstadt, Germany) and a Don Whitley Anaerobic workstation (nitrogen 85%, carbon dioxide 5%, hydrogen 10%). All strains used in this study were grown at 37°C. For a full list of bacteria and their culture conditions used in the antimicrobial spectrum analysis, see Table S1.

Large-scale screen for antimicrobial producers
Fecal samples used in a previous study, 53 which were obtained from a cohort of healthy donors, were used in this study to screen for potential bacteriocinproducing strains active against F. nucleatum DSM15643. These were stored in a BSL-2 laboratory and maintained at −80°C in Teagasc Food Research Center, Moorepark, Fermoy, Ireland. Prior to screening, the samples were removed from storage and defrosted at 37°C in an anaerobic chamber (nitrogen 85%, carbon dioxide 5%, hydrogen 10%, Don Whitley Anaerobic Workstation). Under strict anaerobic conditions, 1 g of fecal matter was serially diluted in sterile phosphate buffered saline (PBS; Sigma Aldrich, Co. Wicklow, Ireland). 100 µl of each dilution was spread on fastidious anaerobe agar (FAA) and grown overnight anaerobically at 37°C. Resulting colonies were overlayed with ~10 ml of FAA containing a 7.5% inoculum of the F. nucleatum DSM15643 and the plates were incubated for a further 18-24 h and subsequently examined for zones of inhibition. Colonies producing distinct zones of inhibition were subcultured onto fresh FAA plates and subsequently stocked in 80% glycerol and stored at −20°C and −80°C for further analysis. Stocked potential bacteriocin-producers were shortlisted by repeat deferred antagonism assays as described and also agar well diffusion assays. 54 For the well assays, molten agar (~45-50°C) was seeded with the F. nucleatum DSM15643 at a seed volume of 3.75%. The inoculated medium was immediately poured into sterile petri dishes and allowed to solidify and dry under anaerobic conditions. Wells of uniform diameter (5.5 mm) were bored in the agar. Aliquots of 50 µl of cell-free supernatant (CFS) from an overnight culture of potential bacteriocin-producers were dispensed into the wells and the plates were incubated overnight for the conditions of the indicator (37°C, anaerobic). pH neutralization of the CFS of the bacteriocin producers was performed by taking 10 ml of fully grown, overnight culture and centrifuging at 4600 rpm for 30 min, the supernatant was then removed and centrifuged again at 4600 rpm for 15 min. The resulting supernatant was then pH adjusted with 1 M NaCl to a pH of ~7.50 µl aliquots of this were dispensed into wells for well diffusion assays as described above. Following incubation, the plates were examined for zones of inhibition around the wells.

Speciation of bacteriocin-producing isolates
Genomic DNA of isolates which produced clear zones of inhibition was extracted from culture cell pellets using the GenElute™ Bacterial Genomic DNA Kit (Sigma-Aldrich; Co. Wicklow, Ireland). Extraction of DNA was confirmed by agarose gel electrophoresis and subsequently the 16S rRNA gene was amplified using the following 16S eubacterial primers CO1; 5'-AGTTTGATCCTCCTGGCTCAG-3' and CO2; 5'-TACCTTGTTACGACTT-3'. 55 The DNA was amplified with Invitrogen Platinum PCR Supermix (ThermoFisher Scientific, Dublin, Ireland) and PCR reactions performed on the Applied Biosystems 2720 Thermocycler (ThermoFisher Scientific, Dublin, Ireland). The amplification cycle used was as follows: 94°C for 2 min, and 30 cycles of the following: 94°C for 30 s, 50°C for 30 s and 72°C for 1.5 min. The purity and quantity of DNA present was checked on the NanoDrop 1000 (ThermoFisher Scientific, Dublin, Ireland) and the PCR product was then purified using the QIAquick™ PCR Purification Kit (Qiagen; Manchester, UK). The complete sequence of the 16S rRNA gene was determined by Sanger sequencing (Beckman Coulter, Essex, UK). The species was putatively identified by comparing the resulting sequence with deposited species in the NCBI database (http://blast.ncbi.nlm.nih.gov/Blast. cgi) with a high percentage nucleotide identity (>98%).

Streptococcus salivarius DPC6993 whole genome sequencing
The purity and concentration of the S. salivarius DPC6993 genomic DNA preparation was confirmed using the NanoDrop 1000 (ThermoFisher Scientific, Dublin, Ireland) and Qubit® 2.0 Fluorometer (ThermoFisher Scientific, Dublin, Ireland) according to the respective manufacturer's protocols. To purify the DNA before beginning the library preparation the Power Clean DNA Cleanup Kit (MO-BIO laboratories; Carlsbad, CA, USA) was used. Genomic libraries were prepared using the Nextera XT Library Preparation kit (Illumina inc., San Diego, CA, USA). Whole genome sequencing was performed using the MiSeq v3 600 cycles Paired Ends kit on the Illumina MiSeq platform (Illumina inc., San Diego, CA, USA) at the Teagasc Food Research Center, Moorepark, Fermoy. The resulting reads were quality checked using FastQC 56 and BBDuk was used to remove sequencing adapters and PhiX reads and perform quality trimming (https://sourceforge.net/projects/ bbmap/). The paired end reads were assembled into contigs and scaffolds using the SPAdes Genome Assembler. 57 Open reading frames of the draft genome were predicted using Prodigal 58 and complementary gene calling and automated annotation was completed using the RAST annotation server. 59 BAGEL3 software, an automated bacteriocin mining tool, was used to detect the presence of any putative bacteriocin operons. 26 Manual analysis of the genome was then subsequently performed using the ARTEMIS genome browser. 60 Manual annotation of the genes potentially involved and surrounding the putative bacteriocin operons was completed by using the BLASTp algorithm and the non-redundant database provided by the NCBI 61 (http://blast.ncbi.nlm.nih.gov).

Colony mass spectrometry
Fully grown colonies of S. salivarius DPC6993 were mixed with 50 µl 2-propanol 0.1% TFA, vortexed three times and centrifuged at 14,000 rpm for 30 s. MALDI TOF mass spectrometry was performed on the cell supernatant using an Axima TOF 2 MALDI-TOF mass spectrometer (Shimadzu Biotech, Manchester, UK). A 0.5 µl aliquot of matrix solution (α-cyano 4-hydroxy cinnamic acid, 10 mg/ml in acetonitrile -0.1% (v/v) TFA) was deposited onto the target and left for 5 s before being removed. The residual solution was allowed to air-dry and 0.5 µl sample solution was deposited onto the pre-coated sample spot. Matrix solution of 0.5 µl was added to the deposited sample and allowed to air-dry. The sample was subsequently analyzed in positive-ion linear mode.

Antimicrobial activity assays
The antimicrobial activity of S. salivarius DPC6993 against F. nucleatum DSM15643 and Lactobacillus delbrueckii subsp. bulgaricus DPC5383 was determined by a deferred antagonism assay 62 in triplicate using three biological replicates. Activity against a range of grampositive and gram-negative gut bacteria (Table  S1) was also assessed. FAA (Lab M, Lancashire, UK) and BHI (Difco Laboratories, Detroit, MI, USA) were used for F. nucleatum DSM15643 and S. salivarius DPC6993, respectively. For the antagonism assay, a fully cultured S. salivarius DPC6993 streak plate was overlayed with 0.75% agar seeded with F. nucleatum DPC6993 (7.5%). For the spot-on lawn assay, 10 µl of an overnight broth culture of S. salivarius DPC6993 was aliquoted onto solid BHI (Difco Laboratories, Detroit, MI, USA) agar and incubated anaerobically at 37°C for 24 h. Subsequently, it was overlayed with FAA (Lab M, Lancashire, UK) seeded with F. nucleatum DSM15643 (7.5%) and examined for evidence of inhibition following overnight incubation.

Donor recruitment for ex vivo colon model experiments
Recruitment and enrollment to the study was sanctioned by the Clinical Research Ethics Committee of the Cork Teaching Hospitals (protocol no. APC091). Informed consent was given by all volunteers, which demonstrated their willingness to donate a fecal sample to the study. All donors were healthy adults over the age of 18, and exclusion criteria included no significant acute or chronic coexisting illness; taking a medication that would interfere with the objectives of the study including anti-inflammatory drugs, corticosteroids, laxatives, enemas, antibiotics (within 3 months), anticoagulants, and overthe-counter nonsteroidal analgesics; has been in a recent experimental trial no less than 30 d prior to commencement of this study; and has a malignant disease or any concomitant endstage organ disease.

Preparation of a frozen standard fecal inoculum and associated medium
The frozen standard fecal inoculum (FSI) was prepared as previously described 49 with minor modifications. Briefly, the FSI was prepared using a total of eight donor fecal samples. Potassium phosphate buffer (50 mM; pH 6.8) was used to resuspend the cell biomass resulting in the fecal slurry preparation. Glycerol was added to a final concentration of 25% and the slurry was frozen at −80°C. The medium used was as previously described 63 and 5% w/v glucose was added to the medium as the carbon source.

Simulation of the human distal colon
The human distal colon environment was simulated using the micro-Matrix (Applikon Biotechnology, Heertjeslaan 2, 2629 JG Delft, Netherlands) as previously described 7 with minor modifications. The micro-Matrix is a mini fermentation system capable of simulating the environmental conditions of the human colon. Multiple treatments were applied using separate colon model wells in a micro-Matrix cassette, assigning three wells per treatment group. The fermentation medium and carbon source were mixed in an anaerobic chamber 2 h before commencement of the trial. Then, 480 µL of thawed FSI was inoculated into each well. S. salivarius DPC6993 adjusted to a concentration of ~10 9 CFU/mL to ensure viability and target the minimum recommended probiotic dose 64 and/or F. nucleatum DSM1564 adjusted to a concentration of ~10 6 CFU/mL to mimic the levels of F. nucleatum in human gut microbiomes (relative abundance of <1%) 40,41,65 was added to each designated well and made up to a final volume of 6 mL using the fermentation medium. Control wells containing just the standardized fecal inoculum and fermentation medium were also included. At Time 0 h (T0), 1 mL was taken from each well of the cassette in the anaerobic chamber to leave a total fermentation volume of 5 mL. The cassette was secured into the micro-Matrix and parts fitted as per the manufacturer's instructions and fermentation parameters including nitrogen gas (40%), CO 2 gas, Orbiter (250 RPM), NaOH, pH (6.8), temperature (37°C) and DO (0%) were as previously described. 7 In addition to thawed SFI and fermentation medium, the cassette was set up with the following colon model treatments: S. salivarius DPC6993 with F. nucleatum DSM15643; S. salivarius DPC6993 only; F. nucleatum DSM15643 only and controls.

DNA extraction from micro-Matrix well samples
At time 0 h (T0), 6 h (T6) and 24 h (T24), 1 mL was taken from each well. Total bacterial metagenomic DNA was extracted from each sample using the Zymo Research ZR fecal DNA kit (Cambridge Biosciences, Cambridge, UK). Each slurry sample was centrifuged at 4000 rpm for 10 min to concentrate the bacterial cells. The supernatant was removed, and cell pellets were frozen at −80°C prior to DNA extraction. The resulting cell biomass was resuspended in lysis buffer and extractions were performed according to the manufacturer's instructions and quantified using the Qubit 2.0 Fluorometer (Life Technologies, Carlsbad, CA, USA) and the purity checked using the NanoDrop 1000 (ThermoFisher Scientific, Dublin, Ireland).

Quantitative PCR
Abundances of F. nucleatum were determined by realtime PCR based on SYBR-Green I fluorescence. 66 Absolute quantification of F. nucleatum was performed using the Roche LightCycler 96 platform. To quantify F. nucleatum, the gene nusG was amplified as previously targeted using F. nucleatum nusG specific primers. 14 There is only one copy of nusG per F. nucleatum genome, and therefore each copy represents a single cell. The primer sequences used were as follows: nusG forward primer, 5'-CAACCATTAC TTTAACTCTACCATGTTCA-3'; nusG reverse primer, 5'-GTTGACTTTACAGAAGGAGATTATG TAAAAATC-3'. BLAST analysis of the primer sequences against the NCBI database confirmed 100% nucleotide identity with the F. nucleatum nusG gene sequences and no other matches of concern were evident. Cycling conditions for the qPCR analysis were as follows: 40 cycles of 94°C for 30 s, 55°C for 30 s and 72°C for 1 min. qPCR samples were performed in triplicate. Each qPCR reaction contained 5 μL KAPA SYBR® FAST (2X) (Merck, Product# KK4610), forward and reverse primer (1 μM), PCR grade water and 1 µl of metagenomic DNA in a total reaction volume of 10 µL. Negative controls comprise PCR-grade water replacing metagenomic DNA. For the quantification of the target gene of interest (GOI), standard curves were generated using serial diluted copies of the GOI using a known DNA template. 66 For quantification of F. nucleatum in colon model samples, standard curves were generated using 10 5 to 10 1 copies of nusG/µL using F. nucleatum DSM15643 as a DNA template with an efficiency of 94% and an R-squared value of >0.99. Standard curves were constructed by plotting the quantification cycle (Ct) values versus the log quantity of the target gene in each dilution series. Colon model metagenomic DNA samples were quantified against the standard curve to obtain absolute quantity of nusG per μg of DNA. The data analysis was performed using the Roche LightCycler 96 real-time PCR system software.

MiSeq compositional sequencing and bioinformatic analysis of sequencing data
Metagenomic DNA extracted from colon model samples were prepared for MiSeq compositional sequencing by 16S rRNA amplification of the V3-V4 variable region of the 16S rRNA gene as described by Illumina Inc. Samples were sequenced using the Illumina MiSeq platform in the Teagasc sequencing facility, Moorepark, Fermoy, Ireland. 16S rRNA amplicon analysis was performed using Qiime2 (v. 2018.11.0). 67 Adapter and primer sequences were removed using cutadapt trimpaired. 68 The dada2 denoise-paired plugin 69 was used to trim forward and reverse reads to 283 and 204 bp, respectively, based on quality score visualization by demux summary, and identify amplicon sequence variants (ASVs), and the ASV phylogenetic tree was calculated using phylogeny align-to-treemafft-fasttree. The 99% identity 16S rRNA rep set of the Silva 132 database 70 was downloaded, and the relevant variable regions were isolated from these full-length 16S rRNA sequences using featureclassifier extract-reads 71 with the primer sequences mentioned above and trimmed to 466 bp based on the median read length of the dataset. These reads were used to train a naïve-Bayes classifier with feature-classifier fit-classifier-naive-Bayes and feature-classifier classify-sklearn 72 was used to assign taxonomy to the ASVs. Qiime2 artifacts were exported in BIOM format 73 and used for downstream analysis.

Statistical analysis
All statistical analysis was computed using R (v3.5.2). The mean quantity of F. nucleatum between colon model treatments was compared with the unpaired t-test. p-values less than 0.05 (p < .05) were accepted as a statistically significant difference between the means. The ggplot2 package (v3.2.1) and GraphPad Prism (v9.0) was used to visualize qPCR and 16S rRNA data. Beta and Alpha diversity calculations were completed using the vegan package (v2.5.6). Adonis analysis was implemented using "Adonis" in the package Vegan. 74 Differences in Alpha diversity metrics were compared using the unpaired t-test.

Author's contributions
GWL wrote the main manuscript. CMG and PDC conceived the study idea and design. GWL, NM, CMG, MB, TMK, and EML designed and set up the experiments. GWL and NM performed the main experiments. CJW ran the bioinformatic pipeline. PMOC performed colony mass spectrometry. CMG, MB and PDC supervised, edited, and proofread the manuscript. All authors read and approved the final manuscript.

Data availability
All metagenomic raw reads have been deposited in ENA under accession number PRJEB49010. The S. salivarius DPC6993 Whole Genome Shotgun project has been deposited at DDBJ/ENA/GenBank under bioproject number PRJNA819233 and accession JALMLR000000000. The version described in this paper is version JALMLR010000000

Disclosure statement
No potential conflict of interest was reported by the author(s).